Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Visilizumab is a humanized, non-Fc receptor (FcR)-binding IgG2 monoclonal antibody directed against the CD3 receptor on activated T cells. Developed by PDL BioPharma, it was investigated as an immunosuppressive agent for immune-mediated diseases such as ulcerative colitis and Crohn's disease. The drug binds to the invariant CD3 epsilon subunit of the T-cell receptor complex on activated T cells, inducing apoptosis predominantly in mucosal CD4+ T lymphocytes via caspase 3 and 8 activation, without affecting resting or peripheral blood T cells. This mechanism aims to rapidly eliminate pathogenic T cells in inflamed tissues while minimizing cytokine release toxicity due to its engineered Fc region that prevents FcR binding. Despite initial promise, clinical development was discontinued after Phase II/III trials due to insufficient efficacy and safety compared with other therapies[1][4][5][6][8].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on visilizumab.